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Cystinose juvénile révélée au stade d’insuffisance rénale chronique terminale

Autor: I. Simon, R. Sava, F. Rasquin, L. Ghisdal, S. Fagnoul, L. Bienfait, I. Houem, Joëlle Nortier

Publikováno v: Néphrologie & Thérapeutique. 14:345

Introduction La cystinose est une maladie autosomique recessive rare liee a une mutation du gene CTNS, codant pour la cystinosine (transporteur lysosomal de cystine). Cette affection s’accompagne d’une accumulation de cystine intra-lysosomale au

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e3e0a68d494312c732a81752d96c869a
https://doi.org/10.1016/j.nephro.2018.07.214

Contents, Vol. 194, 1997

Autor: Y.-Z. Shen, M.-T. Fernández-Figueras, A. Kempinaire, R. Bergman, R. Jaswal, F. Breier, J.L. Lévêque, B. Fazaa, R. Alfonso, A. Verheyen, P.C.M. van de Kerkhof, L. Puig, H.-C. Chiu, R. Ramón, J.-P. Ortonne, M.-H. Chang, U. Hohenleutner, G.K. Bedi, U. Sass, G.B.E. Jemec, P. Dockx, M. Landthaler, R. Caputo, L. Noens, H. Gollnick, M.R. Kamoun, J. André, P. Galand, R.-J. Teng, Y. Miyachi, A.R. Lombardi, S. Verraes, A.M Layton, O. Vanhooteghem, G.E. Piérard, A. Reynaers, A. Vindevoghel, P. Gengoux, R. Friedman-Birnbaum, A. Cooper, V. Bettoli, A. Simonis, D. Roseeuw, M. Baiget, R. Carreño, P. Bruderer, C. Piérard-Franchimont, Z. Al Sarraf, S. Monstrey, C. Decaestecker, F. Purello D’Ambrosio, L. Vandenbossche, R. Feldmann, W. Stolz, H. Degreef, H. Beele, M. Aricò, P. Verplancke, P. Lorea, R. Kiss, T. Ventura-Spagnolo, J.-M. Mascaró, F. Henry, N. Nikkels-Tassoudji, K. Ongenae, G. Pravatà, M. P. De Padova, D. Touma, J.F. Silvestre, Y.-T. Lin, M. Song, M. Gniadecka, G. Noto, J.E. Arrese, W.J. Cunliffe, M. Heenen, R. Strumia, P. Duschet, H. Azzam, A. Sevila, M. Laporte, L.· Ricciardi, I. Eeckhout, D. Kopera, H. Löw-Weiser, M. Corazza, I. Salmon, M. Alegre, F. Rasquin, A. Virgili, H. De Raeve, J.M. de Moragas, A.J. Kanwar, J. Navas, B. Guarneri, J.-V. Berthe, D. Iliev, A. Morell, P. Paquet, J.J. Stene, Tsou Yau, J. Lambert, F. Gschnait, G. De Dobbeleer, M. Lowy, F. Loschiavo, S. Cavicchini, T. Simonart, N. Kiesch, Y. Yokoyama, J. Goens, D. Goldschmidt, F. Benkirane, P. Elsner, A. Shalita, S.P. Cannavò, J.M. Naeyaert, E. Altieri, G. Ghanem, O. Ishikawa, O.L. Fyrand, C. Goossens, N. Renard, J.-M. Lachapelle, L. De Raeve, E. Del Rio, A. Schelfhout, L. Boon, G.P. Thami, J.J. Leyden, A. Vandeveire

Publikováno v: Dermatology. 194:I-V

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::130b757960812da5a576728f780d3777
https://doi.org/10.1159/000246120

[Central serous corticoid and chorioretinopathy]

Autor: F, Rasquin

Publikováno v: Bulletin de la Societe belge d'ophtalmologie. (304)

Central serous chorioretinopathy (CSC) is a relatively frequent ocular disorder. Its pathophysiology remains however unclear. This disease typically affects young men with type A behaviour within a context of stressful events. Recently, endogenous or

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5c9f0080d19091f25ff6480665b35bec
https://pubmed.ncbi.nlm.nih.gov/17718232

Macular CMV retinitis: a case report

Autor: P, Demols, C A, Claes, C M, Farber, F, Rasquin

Publikováno v: Bulletin de la Societe belge d'ophtalmologie. (293)

Cytomegalovirus (CMV) retinitis is the most common ocular opportunistic infection associated with AIDS. It usually affects the peripheral retina, sparing the macula. We describe an atypical CMV retinitis exclusively confined to the macula.A 43-year-o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2c610aa48df1c4e88e03ea4067f3c29e
https://pubmed.ncbi.nlm.nih.gov/15510719